The Toxoplasma gondii virulence factor ROP16 acts in cis and trans, and suppresses T cell responses

被引:46
作者
Chen, Longfei [1 ,2 ]
Christian, David A. [2 ]
Kochanowsky, Joshua A. [3 ,4 ]
Phan, Anthony T. [2 ]
Clark, Joseph T. [2 ]
Wang, Shuai [2 ]
Berry, Corbett [2 ]
Oh, Jung [5 ]
Chen, Xiaoguang [1 ]
Roos, David S. [5 ]
Beiting, Daniel P. [2 ]
Koshy, Anita A. [3 ,4 ]
Hunter, Christopher A. [2 ]
机构
[1] Southern Med Univ, Sch Publ Hlth, Dept Pathogen Biol, Guangzhou, Guangdong, Peoples R China
[2] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
[3] Univ Arizona, BIO5 Inst, Dept Neurol, Tucson, AZ 85724 USA
[4] Univ Arizona, BIO5 Inst, Dept Immunobiol, Tucson, AZ 85724 USA
[5] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
IFN-GAMMA; PPAR-GAMMA; MACROPHAGES; EXPRESSION; INFECTION; OVERPRODUCTION; IMMUNITY; IL-12; PROLIFERATION; TRANSCRIPTION;
D O I
10.1084/jem.20181757
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ability of Toxoplasma gondii to inject the rhoptry kinase ROP16 into host cells results in the activation of the transcription factors STAT3 and STAT6, but it is unclear how these events impact infection. Here, parasites that inject Cre-recombinase with rhoptry proteins were used to distinguish infected macrophages from those only injected with parasite proteins. Transcriptional profiling revealed that injection of rhoptry proteins alone was sufficient to induce an M2 phenotype that is dependent on STAT3 and STAT6, but only infected cells displayed reduced expression of genes associated with antimicrobial activity and protective immunity. In vivo, the absence of STAT3 or STAT6 improved parasite control, while the loss of ROP16 resulted in a marked reduction in parasite numbers and heightened parasite-specific T cell responses. Thus, ROP16 is a virulence factor that can act in cis and trans to promote M2 programs and which limits the magnitude of parasite-specific T cell responses.
引用
收藏
页数:21
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